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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463510Generated: October 29, 2026

Thionyl Chloride → HCID 13300848, compound

https://huagongshe.com/reaction/463510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13300847HCID 13300847—
SolventBenzeneHCID 241—
ProductHCID 13300848HCID 13300848—

Reaction Steps

3-(4(p-trifluoromethylphenoxy)phenyl)-4-phenylbutyric acid (23 g) was refluxed in benzene with thionyl chloride (46 ml) for one hour. The solution was then evaporated to dryness and the residue dissolved in benzene (23 ml). A solution of stannic chloride (23 g) in benzene (46 ml) was added at 0° with stirring. The solution was allowed to stir at 0° for 0.5 hr. Ice; water, diethylether and dilute HCl were then added sequentially. The ether extracts were further washed with aqueous potassium hydroxide and evaporated to give 3-(4-(p-trifluoromethylphenoxy)phenyl)tetralone m.p. 136°-137° (ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04520007
Source datasetuspto-grants-1985_05
ORD IDord-ddca9abd250f4496b7dfd262b8fdeefe
Source noteuspto-grants-1985_05